Epoxy-based stoving enamels comprising carboxyl-functional alkylidenepolyphenols
Stoving enamels comprising epoxy resins and carboxyl-functional alkylidenepolyphenols in a quantity such that the carboxyl groups are present at least in equimolar quantities relative to the epoxide groups of the epoxy resins are suitable for coating the inside of metallic food containers and give, on the packaging, baked coating films which are essentially free from migratable constituents carrying epoxide groups.
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Claims
1. A stoving enamel consisting essentially of one or more epoxy resins containing more than one epoxide group per molecule and one or more carboxyl-functional novolaks which are reaction products of a novolak and one or more acids selected from the group consisting of olefinically unsaturated mono- and dicarboxylic acids, anhydrides of the mono- and dicarboxyclic acids, and haloalkanoic acids,
- in a quantity such that the carboxyl groups are present in at least an equimolar quantity relative to the epoxide groups of the epoxy resins, and the enamel optionally comprising a natural-resin acid.
2. A stoving enamel as claimed in claim 1, wherein the carboxyl-functional novolak comprise a reaction product of one or more novolaks with one or more halocarboxylic acids.
3. A stoving enamel as claimed in claim 1, wherein the carboxyl-functional novolak comprise a reaction product of one or more novolaks with one or more olefinically unsaturated dicarboxylic acids or their anhydrides.
4. A stoving enamel as claimed in claim 1, wherein the carboxyl-functional novolak comprise a reaction product of one or more novolaks, one or more natural-resin acids, and one or more olefinically unsaturated dicarboxylic acids or their anhydrides.
5. A process for the preparation of a stoving enamel as claimed in claim 1, comprising mixing the epoxy resin and carboxyl-functional novolak and then adding an acid catalyst to the mixture.
6. A process as claimed in claim 5, wherein the weight ratio of epoxy resin to carboxyl-functional novolak is from 8.5:1 to 1:4.
7. A process as claimed in claim 5, wherein the acid catalyst comprises phosphoric acid.
8. A method of using the stoving enamel as claimed in claim 1, which comprises coating a food container with the stoving enamel.
9. A method of using the stoving enamel as claimed in claim 1, which comprises coating the inside surface of a metal container with the stoving enamel.
10. A method of using the stoving enamel as claimed in claim 1, Which comprises forming a baked coating film on packaging, which is essentially free from migratable constituents carrying epoxide groups, wherein the coating film comprises the stoving enamel.
11. A stoving enamel as claimed in claim 2, wherein the halocarboxylic acid comprises chloroacetic acid.
12. A stoving enamel as claimed in claim 3, wherein the olefinically unsaturated dicarboxylic and/or anhydride comprises fumaric acid, maleic acid, or maleic acid anhydride.
13. A stoving enamel as claimed in claim 1; wherein the ratio of the novolak to the weight of the carboxylic acid components is (100-x):x, wherein x.ltoreq.40.
14. A stoving enamel as claimed in claim 13, wherein x is from 10 to 20.
15. A stoving enamel as claimed in claim 1, wherein the carboxyl-functionality is provided by fumaric acid, maleic acid, or maleic acid anhydride.
16. A stoving enamel as claimed in claim 1, which further comprises rosin as the natural-resin acid.
17. A product formed by curing the stoving enamel of claim 1.
18. A stoving enamel as claimed in claim 1, wherein the epoxy resin has an epoxide equivalent weight of 100 to 2000 g/mol.
19. A stoving enamel as claimed in claim 1, wherein there is from 1.1 to 10 mol of carboxylic group in the carboxy-functional novolak per mol of epoxide groups in the epoxy resin.
20. A product of claim 17, which is free from migratable constituents carrying epoxy groups.
| 5177161 | January 5, 1993 | Graff et al. |
| 01-146963 | June 1989 | JPX |
| 04-202413 | July 1992 | JPX |
- CAPLUS accession No. 1991:166449 for European application No. 388913, Hoescht A.G., Sep. 1990. Ullmann's Encyclopedia of Industrial Chemistry, "Paintings and Coatings", Fifth, Completely Revised Edition, vol. A18, pp. 359-360. Ullmann's Encyclopedia of Industrial Chemistry,"Paintings and Coatings", Fifth, Completely Revised Edition, vol. A18, pp. 418-421. The Chemistry of Phenolic Resins, "Epoxide Resins", Chapter 5, 1967, pp. 92-100. P. Nylen, "Modern Surface Coatings", 1965, pp. 178-253. W. S. Zimmt, "Coatings from Acrylic Polymers", CHEMTECH, Nov. 1981, pp. 681-683. von William Brushwell, "Einsatz und Modifizierung von Acrylatharzen", Farbe und Lack, 86, 1980, pp. 706-710.
Type: Grant
Filed: May 20, 1996
Date of Patent: Jan 13, 1998
Assignee: Vianova Resins GmbH (Mainz-Kastel)
Inventors: Thomas Burkhart (Mainz), Wolfgang Hesse (Schlangenbad), Paul Oberressl (Wiesbaden)
Primary Examiner: Robert E. Sellers
Law Firm: Foley & Lardner
Application Number: 8/650,773
International Classification: C08L 6114; C08L 6302; C08L 6304;
